Cited by 112SARS-CoV-2 and COVID-19 ResearchEvolution and Genetic DynamicsCOVID-19 epidemiological studies

SARS-CoV-2 Variant of Concern 202012/01 Has about Twofold Replicative Advantage and Acquires Concerning Mutations

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Grabowski, Frederic, Preibisch, Grzegorz, Giziński, Stanisław, Kochańczyk, Marek, Lipniacki, Tomasz·2021·Viruses

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Abstract

The novel SARS-CoV-2 Variant of Concern (VOC)-202012/01 (also known as B.1.1.7), first collected in United Kingdom on 20 September 2020, is a rapidly growing lineage that in January 2021 constituted 86% of all SARS-CoV-2 genomes sequenced in England. The VOC has been detected in 40 out of 46 countries that reported at least 50 genomes in January 2021. We have estimated that the replicative advantage of the VOC is in the range 1.83–2.18 [95% CI: 1.71–2.40] with respect to the 20A.EU1 variant that dominated in England in November 2020, and in range 1.65–1.72 [95% CI: 1.46–2.04] in Wales, Scotland, Denmark, and USA. As the VOC strain will likely spread globally towards fixation, it is important to monitor its molecular evolution. We have estimated growth rates of expanding mutations acquired by the VOC lineage to find that the L18F substitution in spike has initiated a fast growing VOC substrain. The L18F substitution is of significance because it has been found to compromise binding of neutralizing antibodies. Of concern are immune escape mutations acquired by the VOC: E484K, F490S, S494P (in the receptor binding motif of spike) and Q677H, Q675H (in the proximity of the polybasic cleavage site at the S1/S2 boundary). These mutants may hinder efficiency of existing vaccines and expand in response to the increasing after-infection or vaccine-induced seroprevalence.

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  • Several Alpha variant sub-lineages have acquired additional mutations that might increase the risk of reinfection and vaccine failure, including the RBD mutations E484K, F490S and S494P.

    “Several Alpha variant sub-lineages have acquired additional mutations that might increase the risk of reinfection and vaccine failure, including the RBD mutations E484K, F490S and S494P (ref. 158 ).”

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References 24 · Cited by 112

Research works printed but not linked: 1

  1. Sabino, E.C.; Buss, L.F.; Carvalho, M.P.S.; Crispim, M.A.E.; Fraiji, N.A.; Pereira, R.H.M.; Parag, K.V.; da Silva Peixoto, P.; Kraemer, M.U.G.; Oikawa, M.K.; et al. Resurgence of COVID-19 in Manaus, Brazil, despite high seroprevalence. Lancet 2021, 397, 452-455.

Authors
Grabowski, F., Preibisch, G., Giziński, S., Kochańczyk, M., & Lipniacki, T.
Affiliations
  • Institute of Fundamental Technological Research (PL)
  • University of Warsaw (PL)
Corresponding author
  • Kochańczyk, Marek
  • Lipniacki, Tomasz
Venue
Viruses
Publisher
MDPI AG
Published
2021-03-01
Volume
13
Issue
3
Pages
392
ISSN
1999-4915 (ISSN-L)
OpenAlex
W3134363787
Cited by
112
References
24
Citations by year
2026: 1 · 2025: 3 · 2024: 8 · 2023: 16 · 2022: 36 · 2021: 48
FWCI
8.55
Type
journal article
Language
en
Open access
Locations
  • Viruses (publishedVersion, cc-by)
  • medRxiv (acceptedVersion, cc-by-nc-nd)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Funders
Norwegian Financial Mechanism (operated by National Science Centre Poland) (GRIEG-1 2019/34/H/NZ6/00699)
Topics
  • Health Sciences › Medicine › Infectious Diseases › SARS-CoV-2 and COVID-19 Research
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Evolution and Genetic Dynamics
  • Physical Sciences › Mathematics › Modeling and Simulation › COVID-19 epidemiological studies
Keywords
SARS-CoV-2, Alpha variant, spike protein mutations, immune escape mutations, E484K, receptor-binding motif, polybasic cleavage site, vaccine escape, neutralizing antibodies, viral growth rate, molecular evolution
MeSH terms
COVID-19, SARS-CoV-2, Humans, Mutation, Phylogeny, Virus Replication, Amino Acid Motifs, Spike Glycoprotein, Coronavirus

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